Nateglinide 68382-0722
Product NDC
68382-0722- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 27, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA205248
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Nateglinide | 120 mg/1 |
Drug Class
Glinide [EPC]Glinide [EPC]Potassium Channel Antagonists [MoA]
Packaging Options(6)
100 TABLET, FILM COATED in 1 BOTTLE (68382-722-01)
500 TABLET, FILM COATED in 1 BOTTLE (68382-722-05)
30 TABLET, FILM COATED in 1 BOTTLE (68382-722-06)
1000 TABLET, FILM COATED in 1 BOTTLE (68382-722-10)
90 TABLET, FILM COATED in 1 BOTTLE (68382-722-16)
10 BLISTER PACK in 1 CARTON (68382-722-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK